Mutations in CFTR genes are associated with oligoasthenospermia in infertile men undergoing IVF
Author:
Affiliation:
1. Center of Reproductive Medicine Shanxi Women and Children Health Hospital Taiyuan China
Publisher
Wiley
Subject
Urology,Endocrinology,General Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/and.14355
Reference20 articles.
1. Semen quality of young adult ICSI offspring: the first results
2. Genetics of the congenital absence of the vas deferens
3. Next-generation sequencing: toward an increase in the diagnostic yield in patients with apparently idiopathic spermatogenic failure
4. Regulation of male fertility by CFTR and implications in male infertility
5. Missense Mutations in SLC26A8, Encoding a Sperm-Specific Activator of CFTR, Are Associated with Human Asthenozoospermia
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1. DNA methylation patterns in patients with asthenospermia and oligoasthenospermia;BMC Genomics;2024-06-17
2. Discovery of a novel miRNA involved in the regulation of male infertility in zebrafish;Genomics;2024-03
3. Novel Biallelic Mutation c.131G>T in MEI1 Causes Meiotic Arrest and Nonobstructive Azoospermia;Andrologia;2024-01
4. One-step NGS molecular analysis of the CFTR gene on newborn dried blood spots gives a higher diagnostic sensitivity in affected and carrier subjects: A pilot study;Clinica Chimica Acta;2024-01
5. The role of CFTR p.G970D missense mutation in male infertility;Asian Journal of Andrology;2023
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